IP Library Granted Patent US 12,115,143
Granted Patent B2
US 12,115,143 · App. 18/537,342 · Granted Oct 15, 2024

Modified release gamma-hydroxybutyrate formulations having improved pharmacokinetics

Inventors: Jordan Dubow (Lyons, FR); Hervé Guillard (Villeurbanne, FR); Claire Mégret (Lyons, FR); Jean-François Dubuisson (Lyons, FR)
Assignee: Flamel Ireland Limited
A61K31/22A61K9/14A61K9/1676A61K9/5015A61K9/5026A61K9/5042A61K9/5078A61K9/5084A61K31/19
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Quick Facts
Patent No.
US 12,115,143
App. No.
18/537,342
Granted
Oct 15, 2024
Kind
B2
Abstract

Modified release formulations of gamma-hydroxybutyrate having improved dissolution and pharmacokinetic properties are provided, and therapeutic uses thereof.

Claims (50)

1. A pharmaceutical formulation comprising:

an immediate release portion comprising gamma-hydroxybutyrate;

a modified release portion comprising particles, the particles comprising gamma-hydroxybutyrate and a coating, wherein the coating comprises a methacrylic acid and methyl methacrylate copolymer and a methacrylic acid and ethyl acrylate copolymer;

an acidifying agent; and

one or more suspending or viscosifying agents,

wherein the formulation comprises an amount of gamma-hydroxybutyrate equivalent to from 3.0 g to 12.0 g of sodium oxybate, and

wherein the acidifying agent and the one or more suspending or viscosifying agents are not a component of the particles.

2. The pharmaceutical formulation of claim 1 , wherein the formulation is designed to be administered orally only once nightly.

3. The pharmaceutical formulation of claim 1 , wherein the modified release portion comprises hydrogenated vegetable oil.

4. The pharmaceutical formulation of claim 1 , wherein the suspending or viscosifying agents comprise 1% to 15% (w/w) of the formulation.

5. The pharmaceutical formulation of claim 1 , wherein the suspending or viscosifying agents comprise 2% to 10% (w/w) of the formulation.

6. The pharmaceutical formulation of claim 1 , wherein the suspending or viscosifying agents comprise 2% to 5% (w/w) of the formulation.

7. The pharmaceutical formulation of claim 1 , wherein the suspending or viscosifying agents comprise 2% to 3% (w/w) of the formulation.

8. The pharmaceutical formulation of claim 1 , wherein the acidifying agent is selected from the group consisting of malic acid, citric acid, tartaric acid, adipic acid, boric acid, maleic acid, phosphoric acid, ascorbic acid, oleic acid, capric acid, caprylic acid, benzoic acid, and mixtures thereof, and

wherein the one or more suspending or viscosifying agents is selected from the group consisting of xanthan gum, medium viscosity sodium carboxymethyl cellulose, mixtures of microcrystalline cellulose and sodium carboxymethyl cellulose, mixtures of microcrystalline cellulose and guar gum, medium viscosity hydroxyethyl cellulose, agar, sodium alginate, mixtures of sodium alginate and calcium alginate, gellan gum, carrageenan gum grade iota, kappa or lambda, medium viscosity hydroxypropylmethyl cellulose, and mixtures thereof.

9. The pharmaceutical formulation of claim 1 , wherein the coating is 10 to 50% of the weight of the particles.

10. The pharmaceutical formulation of claim 1 , wherein the coating is 15 to 45% of the weight of the particles.

11. The pharmaceutical formulation of claim 1 , wherein the coating is 20 to 40% of the weight of the particles.

12. The pharmaceutical formulation of claim 1 , wherein the coating is 25 to 35% of the weight of the particles.

13. The pharmaceutical formulation of claim 1 , wherein the coating is 30% of the weight of the particles.

14. A pharmaceutical formulation comprising:

an immediate release portion comprising gamma-hydroxybutyrate;

a modified release portion comprising particles, the particles comprising gamma-hydroxybutyrate and a coating, wherein the coating comprises a methacrylic acid and methyl methacrylate copolymer, and a methacrylic acid and ethyl acrylate copolymer;

an acidifying agent selected from the group consisting of malic acid, tartaric acid, and mixtures thereof; and

a suspending or viscosifying agent comprising at least one of carrageenan gum, hydroxyethyl cellulose or xanthan gum,

wherein the acidifying agent and the suspending or viscosifying agent are separate and distinct from the particles.

15. A pharmaceutical formulation comprising:

an immediate release portion comprising gamma-hydroxybutyrate;

a modified release portion comprising particles, the particles comprising gamma-hydroxybutyrate and a coating, wherein the coating comprises a methacrylic acid and methyl methacrylate copolymer, and a methacrylic acid and ethyl acrylate copolymer;

an acidifying agent comprising 1.2% to 15% (w/w) of the formulation; and

one or more suspending or viscosifying agents selected from the group consisting of xanthan gum, sodium carboxymethyl cellulose, mixtures of microcrystalline cellulose and sodium carboxymethyl cellulose, mixtures of microcrystalline cellulose and guar gum, hydroxyethyl cellulose, agar, sodium alginate, mixtures of sodium alginate and calcium alginate, gellan gum, carrageenan gum, hydroxypropylmethyl cellulose, and mixtures thereof,

wherein the acidifying agent and the one or more suspending or viscosifying agents are separate and distinct from the particles.

16. The pharmaceutical formulation of claim 15 , wherein the acidifying agent comprises 1.2% to 10% (w/w) of the formulation.

17. The pharmaceutical formulation of claim 15 , wherein the acidifying agent comprises 1.2% to 5% (w/w) of the formulation.

18. The pharmaceutical formulation of claim 15 , wherein the acidifying agent comprises 1.6% to 3.2% (w/w) of the formulation.

19. The pharmaceutical formulation of claim 15 , wherein the acidifying agent comprises about 1.6% (w/w) of the formulation.

20. The pharmaceutical formulation of claim 15 , wherein the acidifying agent is selected from the group consisting of malic acid, citric acid, tartaric acid, adipic acid, boric acid, maleic acid, phosphoric acid, ascorbic acid, oleic acid, capric acid, caprylic acid, benzoic acid, and mixtures thereof.

21. The pharmaceutical formulation of claim 15 , wherein the acidifying agent comprises malic acid.

22. The pharmaceutical formulation of claim 15 , wherein the acidifying agent consists of malic acid.

23. The pharmaceutical formulation of claim 15 , wherein the acidifying agent comprises tartaric acid.

24. The pharmaceutical formulation of claim 15 , wherein the acidifying agent consists of tartaric acid.

25. The pharmaceutical formulation of claim 15 , wherein the one or more suspending or viscosifying agents comprises at least one of carrageenan gum, hydroxyethyl cellulose, or xanthan gum.

26. A pharmaceutical formulation comprising:

an immediate release portion comprising gamma-hydroxybutyrate; and

a modified release portion comprising particles, the particles comprising gamma-hydroxybutyrate and a coating, wherein the coating comprises:

a polymer carrying free carboxylic groups and having a pH trigger of from 5.5 to 6.97; and

a hydrophobic compound having a melting point equal or greater than 40° C., wherein a weight ratio of the hydrophobic compound to the polymer carrying free carboxylic groups is from 0.4 to 4;

an acidifying agent; and

one or more suspending or viscosifying agents,

wherein the acidifying agent and the one or more suspending or viscosifying agents are not a component of the particles.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2024
From: DUBOW, JORDAN; GUILLARD, HERVÉ; MÉGRET, CLAIRE; DUBUISSON, JEAN-FRANÇOIS
To: FLAMEL IRELAND LIMITED
Reel/Frame 067858/0944 →
Continuity (11)
Continuation 18231581 · Aug 8, 2023
Continuation 18075980 · Dec 6, 2022
Continuation 17497393 · Oct 8, 2021
Continuation In Part 17178117 · Feb 17, 2021
Continuation In Part 16527633 · Jul 31, 2019
Continuation 16281235 · Feb 21, 2019
Continuation 15655924 · Jul 21, 2017
Provisional Application 62474330 · Mar 21, 2017
Provisional Application 62399413 · Sep 25, 2016
Provisional Application 62365812 · Jul 22, 2016
Related Publication 20240173286A1 · May 30, 2024
Cited By (10)
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